X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes.

Added 2785 days ago (13.04.2014)
Authors: Philips AK, Sirén A, Avela K, Somer M, Peippo M, Ahvenainen M, Doagu F, Arvio M, Kääriäinen H, Van Esch H, Froyen G, Haas SA, Hu H, Kalscheuer VM, Järvelä I
PubMed id: 24721225
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